Pravastatin Sodium
- Product NDC
- 50090-6911
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077987
- Marketing category
- ANDA
- Substance
- PRAVASTATIN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6911-0 | 90 TABLET in 1 BOTTLE (50090-6911-0) | 2023-12-12 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pravastatin Sodium | A-S Medication Solutions | 2025-04-25 | HUMAN PRESCRIPTION DRUG LABEL | 11 |